Krt28 Variant Search Result - Rat Genome Database

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56 records found for search term Krt28

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597798129	CV3698490	single nucleotide variant	NM_181535.3(KRT28):c.12A>G (p.Gln4=)	not specified [RCV004936034]	likely benign	17	40799882	40799882	Human		name
156173398	CV2290068	single nucleotide variant	NM_181535.3(KRT28):c.25T>C (p.Ser9Pro)	not specified [RCV004152749]	uncertain significance	17	40799869	40799869	Human		name
405817304	CV3273044	single nucleotide variant	NM_181535.3(KRT28):c.28A>G (p.Arg10Gly)	not specified [RCV004412289]	uncertain significance	17	40799866	40799866	Human		name
407499859	CV3445500	single nucleotide variant	NM_181535.3(KRT28):c.59C>A (p.Ser20Tyr)	not specified [RCV004644468]	uncertain significance	17	40799835	40799835	Human		name
598221903	CV3980344	single nucleotide variant	NM_181535.3(KRT28):c.74A>G (p.Asn25Ser)	not specified [RCV005360891]	likely benign	17	40799820	40799820	Human		name
156246577	CV2219111	single nucleotide variant	NM_181535.3(KRT28):c.101G>C (p.Ser34Thr)	not specified [RCV004087269]	uncertain significance	17	40799793	40799793	Human		name
156151813	CV2307585	single nucleotide variant	NM_181535.3(KRT28):c.167T>C (p.Val56Ala)	not specified [RCV004168012]	likely benign	17	40799727	40799727	Human		name
401743692	CV2684761	single nucleotide variant	NM_181535.3(KRT28):c.127A>T (p.Ser43Cys)	not specified [RCV004293843]	uncertain significance	17	40799767	40799767	Human		name
401867782	CV2777270	single nucleotide variant	NM_181535.3(KRT28):c.125G>A (p.Gly42Glu)	not specified [RCV004354291]	uncertain significance	17	40799769	40799769	Human		name
405817303	CV3273043	single nucleotide variant	NM_181535.3(KRT28):c.232G>A (p.Glu78Lys)	not specified [RCV004412288]	uncertain significance	17	40799662	40799662	Human		name
407459939	CV3445496	single nucleotide variant	NM_181535.3(KRT28):c.164G>A (p.Ser55Asn)	not specified [RCV004633714]	uncertain significance	17	40799730	40799730	Human		name
597798112	CV3698483	single nucleotide variant	NM_181535.3(KRT28):c.146T>C (p.Leu49Ser)	not specified [RCV004936028]	uncertain significance	17	40799748	40799748	Human		name
156137754	CV2210513	single nucleotide variant	NM_181535.3(KRT28):c.464C>G (p.Thr155Ser)	not specified [RCV004089641]	uncertain significance	17	40798986	40798986	Human		name
156376258	CV2210514	single nucleotide variant	NM_181535.3(KRT28):c.874A>G (p.Ile292Val)	not specified [RCV004089642]	uncertain significance	17	40797020	40797020	Human		name
155976049	CV2211342	single nucleotide variant	NM_181535.3(KRT28):c.665C>T (p.Thr222Ile)	not specified [RCV004090266]	uncertain significance	17	40798260	40798260	Human		name
155935731	CV2221810	single nucleotide variant	NM_181535.3(KRT28):c.699G>C (p.Lys233Asn)	not specified [RCV004102842]	uncertain significance	17	40797273	40797273	Human		name
156289309	CV2229896	single nucleotide variant	NM_181535.3(KRT28):c.835G>A (p.Ala279Thr)	not specified [RCV004105447]	uncertain significance	17	40797137	40797137	Human		name
156093156	CV2256725	single nucleotide variant	NM_181535.3(KRT28):c.910A>C (p.Ser304Arg)	not specified [RCV004118894]	uncertain significance	17	40796984	40796984	Human		name
155941885	CV2300977	single nucleotide variant	NM_181535.3(KRT28):c.803C>A (p.Ala268Asp)	not specified [RCV004158149]	likely benign	17	40797169	40797169	Human		name
156305096	CV2305015	single nucleotide variant	NM_181535.3(KRT28):c.911G>C (p.Ser304Thr)	not specified [RCV004168905]	likely benign	17	40796983	40796983	Human		name
155903877	CV2353693	single nucleotide variant	NM_181535.3(KRT28):c.605A>G (p.Glu202Gly)	not specified [RCV004201709]	uncertain significance	17	40798320	40798320	Human		name
156346456	CV2378054	single nucleotide variant	NM_181535.3(KRT28):c.376G>A (p.Gly126Arg)	not specified [RCV004232615]	uncertain significance	17	40799518	40799518	Human		name
329394860	CV2457685	single nucleotide variant	NM_181535.3(KRT28):c.938T>C (p.Leu313Pro)	not specified [RCV004269535]	uncertain significance	17	40796956	40796956	Human		name
329371313	CV2458074	single nucleotide variant	NM_181535.3(KRT28):c.658G>A (p.Glu220Lys)	not specified [RCV004271903]	uncertain significance	17	40798267	40798267	Human		name
401767142	CV2721608	single nucleotide variant	NM_181535.3(KRT28):c.625G>C (p.Asp209His)	not specified [RCV004316113]	uncertain significance	17	40798300	40798300	Human		name
401892600	CV2782068	single nucleotide variant	NM_181535.3(KRT28):c.989T>C (p.Leu330Pro)	not specified [RCV004359066]	uncertain significance	17	40794036	40794036	Human		name
405817305	CV3269211	single nucleotide variant	NM_181535.3(KRT28):c.346A>G (p.Arg116Gly)	not specified [RCV004412290]	uncertain significance	17	40799548	40799548	Human		name
405817306	CV3269212	single nucleotide variant	NM_181535.3(KRT28):c.400G>C (p.Asp134His)	not specified [RCV004412291]	uncertain significance	17	40799494	40799494	Human		name
405817307	CV3269213	single nucleotide variant	NM_181535.3(KRT28):c.604G>A (p.Glu202Lys)	not specified [RCV004412292]	uncertain significance	17	40798321	40798321	Human		name
405817308	CV3269214	single nucleotide variant	NM_181535.3(KRT28):c.908G>A (p.Arg303Gln)	not specified [RCV004412293]	uncertain significance	17	40796986	40796986	Human		name
405817309	CV3269215	single nucleotide variant	NM_181535.3(KRT28):c.924G>C (p.Glu308Asp)	not specified [RCV004412294]	uncertain significance	17	40796970	40796970	Human		name
405817310	CV3269216	single nucleotide variant	NM_181535.3(KRT28):c.932G>T (p.Arg311Leu)	not specified [RCV004412295]	uncertain significance	17	40796962	40796962	Human		name
405817311	CV3269217	single nucleotide variant	NM_181535.3(KRT28):c.977C>A (p.Thr326Lys)	not specified [RCV004412296]	uncertain significance	17	40796917	40796917	Human		name
407459936	CV3445495	single nucleotide variant	NM_181535.3(KRT28):c.419A>G (p.Tyr140Cys)	not specified [RCV004633713]	uncertain significance	17	40799475	40799475	Human		name
407459943	CV3445497	single nucleotide variant	NM_181535.3(KRT28):c.561A>T (p.Gln187His)	not specified [RCV004633715]	uncertain significance	17	40798364	40798364	Human		name
407499854	CV3445499	single nucleotide variant	NM_181535.3(KRT28):c.734T>C (p.Val245Ala)	not specified [RCV004644467]	uncertain significance	17	40797238	40797238	Human		name
597798115	CV3698484	single nucleotide variant	NM_181535.3(KRT28):c.727G>A (p.Val243Met)	not specified [RCV004936029]	uncertain significance	17	40797245	40797245	Human		name
597798118	CV3698485	single nucleotide variant	NM_181535.3(KRT28):c.754G>C (p.Gly252Arg)	not specified [RCV004936030]	uncertain significance	17	40797218	40797218	Human		name
597798121	CV3698487	single nucleotide variant	NM_181535.3(KRT28):c.744C>G (p.Asn248Lys)	not specified [RCV004936031]	uncertain significance	17	40797228	40797228	Human		name
597798124	CV3698488	single nucleotide variant	NM_181535.3(KRT28):c.518A>G (p.Asp173Gly)	not specified [RCV004936032]	uncertain significance	17	40798932	40798932	Human		name
598221909	CV3980345	single nucleotide variant	NM_181535.3(KRT28):c.314G>A (p.Arg105Gln)	not specified [RCV005360892]	uncertain significance	17	40799580	40799580	Human		name
598184167	CV3980346	single nucleotide variant	NM_181535.3(KRT28):c.794A>G (p.Glu265Gly)	not specified [RCV005353026]	uncertain significance	17	40797178	40797178	Human		name
156237717	CV2193582	single nucleotide variant	NM_181535.3(KRT28):c.1366G>A (p.Gly456Ser)	not specified [RCV004073055]	uncertain significance	17	40792456	40792456	Human		name
156255332	CV2277502	single nucleotide variant	NM_181535.3(KRT28):c.1304G>A (p.Arg435His)	not specified [RCV004145194]	uncertain significance	17	40792518	40792518	Human		name
156149826	CV2307435	single nucleotide variant	NM_181535.3(KRT28):c.1343A>G (p.Glu448Gly)	not specified [RCV004166103]	uncertain significance	17	40792479	40792479	Human		name
156270503	CV2315544	single nucleotide variant	NM_181535.3(KRT28):c.1213A>G (p.Lys405Glu)	not specified [RCV004169590]	uncertain significance	17	40793194	40793194	Human		name
156228698	CV2397590	single nucleotide variant	NM_181535.3(KRT28):c.1175G>A (p.Arg392His)	not specified [RCV004237049]	likely benign	17	40793850	40793850	Human		name
329384646	CV2435159	single nucleotide variant	NM_181535.3(KRT28):c.1027A>G (p.Thr343Ala)	not specified [RCV004252798]	likely benign	17	40793998	40793998	Human		name
405817300	CV3273040	single nucleotide variant	NM_181535.3(KRT28):c.1004C>T (p.Thr335Ile)	not specified [RCV004412285]	uncertain significance	17	40794021	40794021	Human		name
405817301	CV3273041	single nucleotide variant	NM_181535.3(KRT28):c.1025G>A (p.Cys342Tyr)	not specified [RCV004412286]	uncertain significance	17	40794000	40794000	Human		name
405817302	CV3273042	single nucleotide variant	NM_181535.3(KRT28):c.1166C>T (p.Thr389Ile)	not specified [RCV004412287]	uncertain significance	17	40793859	40793859	Human		name
407499851	CV3445498	single nucleotide variant	NM_181535.3(KRT28):c.1336A>G (p.Ile446Val)	not specified [RCV004644466]	uncertain significance	17	40792486	40792486	Human		name
597798127	CV3698489	single nucleotide variant	NM_181535.3(KRT28):c.1376A>C (p.Glu459Ala)	not specified [RCV004936033]	uncertain significance	17	40792446	40792446	Human		name
598162902	CV3980342	single nucleotide variant	NM_181535.3(KRT28):c.1064T>C (p.Leu355Pro)	not specified [RCV005368732]	uncertain significance	17	40793961	40793961	Human		name
598184160	CV3980343	single nucleotide variant	NM_181535.3(KRT28):c.1303C>T (p.Arg435Cys)	not specified [RCV005353025]	uncertain significance	17	40792519	40792519	Human		name
8636139	CV91363	single nucleotide variant	NM_181535.3(KRT28):c.1019A>G (p.Asn340Ser)	Malignant melanoma [RCV000071461]	not provided	17	40794006	40794006	Human		name

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